Disease #03796 (ECTD11B (dysplasia, ectodermal, type 11B, hypohidrotic/hair/tooth, autosomal recessive (ECTD11B)), OMIM:614941)

Official abbreviation ECTD11B
Name dysplasia, ectodermal, type 11B, hypohidrotic/hair/tooth, autosomal recessive (ECTD11B)
OMIM ID 614941
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene EDARADD
Associated tissues -
Disease features -
Remarks -